Park Min Sik, Ma Sang Bok, Lee Dong Joon, Im Dongmin, Doo Seok-Gwang, Yamamoto Osamu
1] Energy Lab., Samsung Advanced Institute of Technology, Samsung Electronics, 130 Samsung-ro, Suwon, Gyeonggi-do 443-803, Republic of Korea [2].
Energy Lab., Samsung Advanced Institute of Technology, Samsung Electronics, 130 Samsung-ro, Suwon, Gyeonggi-do 443-803, Republic of Korea.
Sci Rep. 2014 Jan 22;4:3815. doi: 10.1038/srep03815.
Lithium metal has shown a lot of promise for use as an anode material in rechargeable batteries owing to its high theoretical capacity. However, it does not meet the cycle life and safety requirements of rechargeable batteries owing to electrolyte decomposition and dendrite formation on the surfaces of the lithium anodes during electrochemical cycling. Here, we propose a novel electrolyte system that is relatively stable against lithium metal and mitigates dendritic growth. Systematic design methods that combined simulations, model-based experiments, and in situ analyses were employed to design the system. The reduction potential of the solvent, the size of the salt anions, and the viscosity of the electrolyte were found to be critical parameters determining the rate of dendritic growth. A lithium metal anode in contact with the designed electrolyte exhibited remarkable cyclability (more than 100 cycles) at a high areal capacity of 12 mAh cm(-2).
由于锂金属具有较高的理论容量,它在用作可充电电池的负极材料方面展现出了巨大潜力。然而,在电化学循环过程中,锂负极表面会发生电解质分解和枝晶形成的现象,导致其无法满足可充电电池的循环寿命和安全要求。在此,我们提出了一种新型电解质体系,该体系对锂金属相对稳定,并能减轻枝晶生长。我们采用了结合模拟、基于模型的实验和原位分析的系统设计方法来设计该体系。结果发现,溶剂的还原电位、盐阴离子的大小以及电解质的粘度是决定枝晶生长速率的关键参数。与设计的电解质接触的锂金属负极在12 mAh cm⁻²的高面积容量下表现出了卓越的循环稳定性(超过100次循环)。